C2677565[trait identifier] AND "Suna and Inan Kirac Foundation Neurode - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 873205	NM_007375.4(TARDBP):c.893G>T (p.Gly298Val)	TARDBP (G298V)	Single nucleotide variant (missense variant)	Amyotrophic lateral sclerosis type 10 +1 more	GConflicting classifications of pathogenicity
Select item 5236	NM_007375.4(TARDBP):c.943G>A (p.Ala315Thr)	TARDBP	Single nucleotide variant (missense variant)	Amyotrophic lateral sclerosis type 10 +1 more	GPathogenic
Select item 5234	NM_007375.4(TARDBP):c.1042G>T (p.Gly348Cys)	TARDBP	Single nucleotide variant (missense variant)	not provided +2 more	GPathogenic/Likely pathogenic
Select item 873228	NM_007375.4(TARDBP):c.1060C>G (p.Gln354Glu)	TARDBP (Q354E)	Single nucleotide variant (missense variant)	Amyotrophic lateral sclerosis type 10	GLikely pathogenic
Select item 2501300	NM_007375.4(TARDBP):c.1133A>G (p.Asn378Ser)	TARDBP (N378S)	Single nucleotide variant (missense variant)	Amyotrophic lateral sclerosis type 10	GLikely pathogenic
Select item 21474	NM_007375.4(TARDBP):c.1144G>A (p.Ala382Thr)	TARDBP	Single nucleotide variant (missense variant)	TARDBP-related condition +3 more	GPathogenic/Likely pathogenic
Select item 21476	NM_007375.4(TARDBP):c.1147A>G (p.Ile383Val)	TARDBP (I383V)	Single nucleotide variant (missense variant)	TARDBP-related frontotemporal dementia +3 more	GPathogenic/Likely pathogenic

ClinVar